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Results: 1 to 6 of 6

Tests names and labsConditionsGenes, analytes, and microbesMethods

TUBB - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Symmetric circumferential skin creases, congenital, 1, 156610, Autosomal dominant; CSCSC1 (Multiple benign circumferential skin creases on limbs) (TUBB gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Symmetric circumferential skin creases, congenital, 1, 156610, Autosomal dominant; CSCSC1 (Multiple benign circumferential skin creases on limbs) (TUBB gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

TUBB

Institute for Human Genetics University Medical Center Freiburg
Germany
21
  • C Sequence analysis of the entire coding region

Skin creases, congenital symmetric circumferential: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
22
  • C Sequence analysis of the entire coding region

Microcephaly

Asper Biogene Asper Biogene LLC
Estonia
11196
  • C Sequence analysis of the entire coding region

Results: 1 to 6 of 6

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